In a chemical analysis, the internal standard method involves adding the same amount of a chemical substance to each sample and calibration solution. The internal standard responds proportionally to changes in the analyte and provides a similar, but not identical, measurement signal. It must also be absent from the sample matrix to ensure there is no other source of the internal standard present. Taking the ratio of analyte signal to internal standard signal and plotting it against the analyte concentrations in the calibration solutions will result in a calibration curve. The calibration curve can then be used to calculate the analyte concentration in an unknown sample.[1]

Selecting an appropriate internal standard accounts for random and systematic sources of uncertainty that arise during sample preparation or instrument fluctuation. This is because the ratio of analyte relative to the amount of internal standard is independent of these variations. If the measured value of the analyte is erroneously shifted above or below the actual value, the internal standard measurements should shift in the same direction.[1]

Ratio plot provides good way of compensation of detector sensitivity variation, but may be biased and should be replaced by Relative concentration/Relative calibration calculations if the reason of response variability is in different mass of analysed sample and traditional (not internal standard) calibration curve of any analyte is not linear through origin.[2]

History

The earliest recorded use of the internal standard method dates back to Gouy's flame spectroscopy work in 1877, where he used an internal standard to determine if the excitation in his flame was consistent.[3][4] His experimental procedure was later reintroduced in the 1940s, when recording flame photometers became readily available.[3] The use of internal standards continued to grow, being applied to a wide range of analytical techniques including nuclear magnetic resonance (NMR) spectroscopy, chromatography, and inductively coupled plasma spectroscopy.

Applications

Nuclear magnetic resonance spectroscopy

In NMR spectroscopy, e.g. of the nuclei 1H, 13C and 29Si, frequencies depend on the magnetic field, which is not the same across all experiments. Therefore, frequencies are reported as relative differences to tetramethylsilane (TMS), an internal standard that George Tiers proposed in 1958 and that the International Union of Pure and Applied Chemistry has since endorsed.[5][6] The relative difference to TMS is called chemical shift.[7]

TMS works as an ideal standard because it is relatively inert and its identical methyl protons produce a strong upfield signal, isolated from most other protons.[7] It is soluble in most organic solvents and is removable via distillation due to its low boiling point.[8]

In practice, the difference between the signals of common solvents and TMS are known. Therefore, no TMS needs to be added to commercial deuterated solvents, as modern instruments are capable of detecting the small quantities of protonated solvent present. By specifying the lock solvent to be used, modern spectrometers are able to correctly reference the sample; in effect, the solvent itself serves as the internal standard.[8]

Chromatography

In chromatography, internal standards are used to determine the concentration of other analytes by calculating response factor. The selected internal standard should have a similar retention time and derivatization. It must be stable and not interfere with the sample components. This mitigates the uncertainty that can occur in preparatory steps such as sample injection.[9]

In gas chromatography-mass spectrometry (GC-MS), deuterated compounds with similar structures to the analyte commonly act as effective internal standards.[10] However, there are non-deuterated internal standards such as norleucine, which is popular in the analysis of amino acids because it can be separated from accompanying peaks.[11][12][13]

Selecting an internal standard for liquid chromatography-mass spectrometry (LC-MS) depends on the employed ionization method. The internal standard needs a comparable ionization response and fragmentation pattern to the analyte.[14] LC-MS internal standards are often isotopically analogous to the structure of the analyte, using isotopes such as deuterium (2H), 13C, 15N and 18O.[15]

Inductively coupled plasma

Selecting an internal standard in inductively coupled plasma spectroscopy can be difficult, because signals from the sample matrix can overlap with the those belonging to the analyte. Yttrium is a common internal standard that is naturally absent in most samples. It has both a mid-range mass and emission lines that don't interfere with many analytes. The intensity of the yttrium signal is what the signal from the analyte gets compared to.[16][17]

In Inductively coupled plasma-mass spectrometry (ICP-MS), species with a similar mass to the analyte usually serve as good internal standards, though not in every case. Factors that also contribute to the effectiveness of an internal standard in ICP-MS include how close its ionization potential, change in enthalpy, and change in entropy are to the analyte.[18]

Inductively coupled plasma-optical emission spectroscopy (ICP-OES) internal standards can be selected by observing how the analyte and internal standard signals change with varying experimental conditions. This includes making adjustments to the sample matrix or instrumentation settings and evaluating whether the selected internal standard is reacting in the same way the analyte is.[19]

Example of internal standard method

Spreadsheet for worked-example of plotting nickel concentrations in calibration solutions. The calibration curve on the top does not use the internal standard method. The calibration curve on the bottom does use the internal standard method.

One way to visualize the internal standard method is to create one calibration curve that doesn't use the method and one calibration curve that does. Suppose there are known concentrations of nickel in a set of calibration solutions: 0 ppm, 1.6 ppm, 3.2 ppm, 4.8 ppm, 6.4 ppm, and 8 ppm. Each solution also has 5 ppm yttrium to act as an internal standard. If these solutions are measured using ICP-OES, the intensity of the yttrium signal should be consistent across all solutions. If not, the intensity of the nickel signal is likely imprecise as well.

The calibration curve that does not use the internal standard method ignores the uncertainty between measurements. The coefficient of determination (R2) for this plot is 0.9985.

In the calibration curve that uses the internal standard, the y-axis is the ratio of the nickel signal to the yttrium signal. This ratio is unaffected by uncertainty in the nickel measurements, as it should affect the yttrium measurements in the same way. This results in a higher R2, 0.9993.

References

  1. 1 2 Skoog, Douglas A. (2018). Principles of instrumental analysis. F. James Holler, Stanley R. Crouch (7th ed.). Australia. ISBN 978-1-305-57721-3. OCLC 986919158.{{cite book}}: CS1 maint: location missing publisher (link)
  2. ↑ Kalambet, Yuri; Kozmin, Yuri (18 December 2018). "Internal standard arithmetic implemented as relative concentration/relative calibration". Journal of Chemometrics. 33 (6): 1–7. doi:10.1002/cem.3106.
  3. 1 2 Burns, D. Thorburn; Walker, Michael J. (2019-05-01). "Origins of the method of standard additions and of the use of an internal standard in quantitative instrumental chemical analyses". Analytical and Bioanalytical Chemistry. 411 (13): 2749–2753. doi:10.1007/s00216-019-01754-w. ISSN 1618-2650. PMC 6522454. PMID 30941480.
  4. ↑ Gouy, M. (1880). "Recherches photométriques sur les flammes colorée". Journal de Physique Théorique et Appliquée (in French). 9 (1): 19–27. doi:10.1051/jphystap:01880009001901. ISSN 0368-3893. S2CID 178492346.
  5. ↑ Tiers, George Van Dyke (1958-09-01). "Reliable Proton Nuclear Resonance Shielding Values by "Internal Referencing" with Tetramethyl-silane". The Journal of Physical Chemistry. 62 (9): 1151–1152. doi:10.1021/j150567a041. ISSN 0022-3654.
  6. ↑ Harris, Robin K.; Becker, Edwin D.; Cabral de Menezes, Sonia M.; Goodfellow, Robin; Granger, Pierre (2001-01-01). "NMR nomenclature. Nuclear spin properties and conventions for chemical shifts(IUPAC Recommendations 2001)". Pure and Applied Chemistry. 73 (11): 1795–1818. doi:10.1351/pac200173111795. ISSN 1365-3075. S2CID 95765050.
  7. 1 2 Guzman, Alexander L.; Hoye, Thomas R. (2022-01-21). "TMS is Superior to Residual C H Cl 3 for Use as the Internal Reference for Routine 1 H NMR Spectra Recorded in CDCl 3". The Journal of Organic Chemistry. 87 (2): 905–909. doi:10.1021/acs.joc.1c02590. ISSN 0022-3263. PMID 34974707. S2CID 245651135.
  8. 1 2 Skoog, Douglas A. (2018). Principles of instrumental analysis. F. James Holler, Stanley R. Crouch (7th ed.). Australia. ISBN 978-1-305-57721-3. OCLC 986919158.{{cite book}}: CS1 maint: location missing publisher (link)
  9. ↑ Skoog, Douglas A. (2018). Principles of instrumental analysis. F. James Holler, Stanley R. Crouch (7th ed.). Australia. ISBN 978-1-305-57721-3. OCLC 986919158.{{cite book}}: CS1 maint: location missing publisher (link)
  10. ↑ Unice, Kenneth M.; Kreider, Marisa L.; Panko, Julie M. (2012-11-08). "Use of a Deuterated Internal Standard with Pyrolysis-GC/MS Dimeric Marker Analysis to Quantify Tire Tread Particles in the Environment". International Journal of Environmental Research and Public Health. 9 (11): 4033–4055. doi:10.3390/ijerph9114033. ISSN 1660-4601. PMC 3524611. PMID 23202830.
  11. ↑ Fico, D.; Margapoti, E.; Pennetta, A.; De Benedetto, G. E. (2018-04-01). "An Enhanced GC/MS Procedure for the Identification of Proteins in Paint Microsamples". Journal of Analytical Methods in Chemistry. 2018: e6032084. doi:10.1155/2018/6032084. ISSN 2090-8865. PMC 5902064. PMID 29805835.
  12. ↑ Pons, Alexandre; Richet, Colette; Robbe, Catherine; Herrmann, Annkatrin; Timmerman, Philippe; Huet, Guillemette; Leroy, Yves; Carlstedt, Ingemar; Capon, Calliope; Zanetta, Jean-Pierre (2003-07-01). "Sequential GC/MS Analysis of Sialic Acids, Monosaccharides, and Amino Acids of Glycoproteins on a Single Sample as Heptafluorobutyrate Derivatives". Biochemistry. 42 (27): 8342–8353. doi:10.1021/bi034250e. ISSN 0006-2960. PMID 12846583.
  13. ↑ Harduf, Z.; Bielorai, R.; Alumot, E. (1977-09-11). "Norleucine —an internal standard for the basic column used in physiological amino acid analysis". Journal of Chromatography A. 139 (1): 215–217. doi:10.1016/S0021-9673(01)84148-0. ISSN 0021-9673. PMID 893614.
  14. ↑ "Internal Standard an Important Analyte Use in Drug Analysis by Liquid Chromatography Mass Spectrometry- An Article | International Journal of Pharmaceutical and Bio Medical Science". 2022-01-13. doi:10.47191/ijpbms/v2-i1-02. S2CID 245957199. {{cite journal}}: Cite journal requires |journal= (help)
  15. ↑ Grocholska, Paulina; Bąchor, Remigiusz (2021-05-18). "Trends in the Hydrogen−Deuterium Exchange at the Carbon Centers. Preparation of Internal Standards for Quantitative Analysis by LC-MS". Molecules. 26 (10): 2989. doi:10.3390/molecules26102989. ISSN 1420-3049. PMC 8157363. PMID 34069879.
  16. ↑ Skoog, Douglas A. (2018). Principles of instrumental analysis. F. James Holler, Stanley R. Crouch (7th ed.). Australia. ISBN 978-1-305-57721-3. OCLC 986919158.{{cite book}}: CS1 maint: location missing publisher (link)
  17. ↑ Zachariadis, G. A.; Vogiatzis, C. (2010-05-17). "An Overview of the Use of Yttrium for Internal Standardization in Inductively Coupled Plasma–Atomic Emission Spectrometry". Applied Spectroscopy Reviews. 45 (3): 220–239. Bibcode:2010ApSRv..45..220Z. doi:10.1080/05704921003719122. ISSN 0570-4928. S2CID 98458774.
  18. ↑ Finley-Jones, Haley J.; Molloy, John L.; Holcombe, James A. (2008-08-06). "Choosing internal standards based on a multivariate analysis approach with ICP(TOF)MS". Journal of Analytical Atomic Spectrometry. 23 (9): 1214–1222. doi:10.1039/B804048F. ISSN 1364-5544.
  19. ↑ Sedcole, J. R.; Lee, J.; Pritchard, M. W. (1986-01-01). "Internal standard selection in the presence of matrix interactions in an inductively coupled argon plasma optimised for simultaneous multielement analysis by atomic emission spectrometry". Spectrochimica Acta Part B: Atomic Spectroscopy. 41 (3): 227–235. Bibcode:1986AcSpe..41..227S. doi:10.1016/0584-8547(86)80162-8. ISSN 0584-8547.
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